Canonical Allele Identifier: CA2838267981
Gene: PPM1H HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.62731401C>A , CM000674.2:g.62731401C>A GRCh38
NC_000012.11:g.63125181C>A , CM000674.1:g.63125181C>A GRCh37
NC_000012.10:g.61411448C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000228705.7:c.954+6101G>T MANE Select ENSP00000228705.5:n.954+6101G>T
ENST00000228705.6:c.954+6101G>T ENSP00000228705.5:n.954+6101G>T
ENST00000551519.1:n.344+6101G>T
NM_020700.1:c.954+6101G>T NP_065751.1:n.954+6101G>T
XM_011538578.1:c.840+6101G>T XP_011536880.1:n.840+6101G>T
XM_011538579.1:c.201+6101G>T XP_011536881.1:n.201+6101G>T
XM_011538578.2:c.840+6101G>T XP_011536880.1:n.840+6101G>T
XM_017019676.2:c.954+6101G>T XP_016875165.1:n.954+6101G>T
NM_020700.2:c.954+6101G>T MANE Select NP_065751.1:n.954+6101G>T